Canonical Allele Identifier: CA1565681242
Gene: LNPEP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.97015012A= , CM000667.2:g.97015012A= GRCh38
NC_000005.9:g.96350716A= , CM000667.1:g.96350716A= GRCh37
NC_000005.8:g.96376472A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000231368.10:c.2293A= MANE Select ENSP00000231368.5:p.Ile765=
ENST00000231368.9:c.2293A= ENSP00000231368.5:p.Ile765=
ENST00000395770.3:c.2251A= ENSP00000379117.3:p.Ile751=
NM_005575.2:c.2293A= NP_005566.2:p.Ile765=
NM_175920.3:c.2251A= NP_787116.2:p.Ile751=
XM_024446045.1:c.2293A= XP_024301813.1:p.Ile765=
NM_005575.3:c.2293A= MANE Select NP_005566.2:p.Ile765=
NM_175920.4:c.2251A= NP_787116.2:p.Ile751=